PL2693881T3 - Podstawione analogi N-fenylopirymidyno-2-aminy jako inhibitory kinazy AXL - Google Patents
Podstawione analogi N-fenylopirymidyno-2-aminy jako inhibitory kinazy AXLInfo
- Publication number
- PL2693881T3 PL2693881T3 PL12763555T PL12763555T PL2693881T3 PL 2693881 T3 PL2693881 T3 PL 2693881T3 PL 12763555 T PL12763555 T PL 12763555T PL 12763555 T PL12763555 T PL 12763555T PL 2693881 T3 PL2693881 T3 PL 2693881T3
- Authority
- PL
- Poland
- Prior art keywords
- phenylpyrimidin
- inhibitors
- substituted
- axl kinase
- amine analogs
- Prior art date
Links
- 108091000080 Phosphotransferase Proteins 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- DWTIGFGVHORZND-UHFFFAOYSA-N n-phenylpyrimidin-2-amine Chemical class N=1[C]=CC=NC=1NC1=CC=CC=C1 DWTIGFGVHORZND-UHFFFAOYSA-N 0.000 title 1
- 102000020233 phosphotransferase Human genes 0.000 title 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/48—Two nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161471090P | 2011-04-01 | 2011-04-01 | |
| EP12763555.5A EP2693881B1 (fr) | 2011-04-01 | 2012-03-31 | Analogues de n-phénylpyrimidine-2-amine substitués en tant qu'inhibiteurs de l'axl kinase |
| PCT/US2012/031768 WO2012135800A1 (fr) | 2011-04-01 | 2012-03-31 | Analogues de n-phénylpyrimidine-2-amine substitués en tant qu'inhibiteurs de l'axl kinase |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL2693881T3 true PL2693881T3 (pl) | 2020-03-31 |
Family
ID=46931967
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL12763555T PL2693881T3 (pl) | 2011-04-01 | 2012-03-31 | Podstawione analogi N-fenylopirymidyno-2-aminy jako inhibitory kinazy AXL |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US8901120B2 (fr) |
| EP (2) | EP3628665B1 (fr) |
| JP (2) | JP6118794B2 (fr) |
| BR (1) | BR112013025387B1 (fr) |
| CY (1) | CY1122556T1 (fr) |
| DK (1) | DK2693881T3 (fr) |
| ES (2) | ES2937952T3 (fr) |
| HU (1) | HUE046988T2 (fr) |
| PL (1) | PL2693881T3 (fr) |
| PT (1) | PT2693881T (fr) |
| WO (1) | WO2012135800A1 (fr) |
Families Citing this family (52)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MX2011008362A (es) | 2009-02-13 | 2011-08-24 | Shionogi & Co | Derivado novedoso de triazina y composicion farmaceutica que comprende el mismo. |
| EP3521291A1 (fr) | 2010-05-20 | 2019-08-07 | Array Biopharma, Inc. | Composés macrocycliques comme inhibiteurs de la kinase trk |
| RU2565073C2 (ru) | 2010-08-10 | 2015-10-20 | Сионоги Энд Ко., Лтд. | Триазиновое производное и включающая его фармацевтическая композиция, обладающая анальгетической активностью |
| JP6075621B2 (ja) | 2010-08-10 | 2017-02-08 | 塩野義製薬株式会社 | 新規複素環誘導体およびそれらを含有する医薬組成物 |
| WO2012135800A1 (fr) | 2011-04-01 | 2012-10-04 | University Of Utah Research Foundation | Analogues de n-phénylpyrimidine-2-amine substitués en tant qu'inhibiteurs de l'axl kinase |
| EP2694486B1 (fr) | 2011-04-01 | 2018-01-10 | University of Utah Research Foundation | Analogues de n-(3-(pyrimidine-4-yl)phényl)acrylamide substitués en tant qu'inhibiteurs du récepteur tyrosine kinase btk |
| US9550763B2 (en) | 2012-02-09 | 2017-01-24 | Shionogi & Co., Ltd. | Heterocyclic ring and carbocyclic derivative |
| KR20150067298A (ko) | 2012-10-04 | 2015-06-17 | 유니버시티 오브 유타 리서치 파운데이션 | 티로신 수용체 키나아제 btk 억제제로서의 치환된 n-(3-(피리미딘-4-일)페닐)아크릴아미드 유사체 |
| CA2887435A1 (fr) | 2012-10-04 | 2014-04-10 | University Of Utah Research Foundation | Analogues de n-(3-(pyrimidin-4-yl)phenyl) substitue utilises en tant qu'inhibiteurs de recepteur tyrosine kinase btk |
| CA2905993C (fr) | 2013-03-14 | 2022-12-06 | Tolero Pharmaceuticals, Inc. | Derives de 4-amino-pyrimidinyle-2-amino-phenyle substitues et compositions pharmaceutiques a base de ceux-ci en tant qu'inhibiteurs dejak2 et d'alk2 |
| TWI637949B (zh) | 2013-06-14 | 2018-10-11 | 塩野義製藥股份有限公司 | 胺基三衍生物及含有其等之醫藥組合物 |
| WO2015077375A1 (fr) | 2013-11-20 | 2015-05-28 | Signalchem Lifesciences Corp. | Dérivés de quinazoline servant d'inhibiteurs des kinases de la famille tam |
| KR102398473B1 (ko) | 2013-11-27 | 2022-05-16 | 시그널켐 라이프사이언시즈 코포레이션 | Tam 패밀리 키나제 억제제로서의 아미노피리딘 유도체 |
| US9840503B2 (en) | 2015-05-11 | 2017-12-12 | Incyte Corporation | Heterocyclic compounds and uses thereof |
| KR20180041135A (ko) | 2015-07-16 | 2018-04-23 | 어레이 바이오파마 인크. | Ret 키나아제 억제제로서 치환된 피라졸로[1,5-a]피리딘 화합물 |
| WO2017024019A1 (fr) * | 2015-08-04 | 2017-02-09 | Celgene Corporation | Procédés de traitement de la leucémie lymphocytaire chronique et utilisation de biomarqueurs en tant que prédicteur de sensibilité clinique à des thérapies immunomodulatrices |
| WO2017027717A1 (fr) | 2015-08-12 | 2017-02-16 | Incyte Corporation | Composés de pyrimidine fusionnés bicycliques utilisés en tant qu'inhibiteurs de tam |
| WO2017035366A1 (fr) | 2015-08-26 | 2017-03-02 | Incyte Corporation | Dérivés de type pyrrolo-pyrimidine utilisés comme inhibiteurs des tam |
| IL298653A (en) * | 2015-12-11 | 2023-01-01 | Immatics Biotechnologies Gmbh | New peptides and a combination of peptides for use in immunotherapy against several types of cancer |
| JP6885390B2 (ja) | 2016-02-26 | 2021-06-16 | 小野薬品工業株式会社 | Ａｘｌ阻害剤と免疫チェックポイント阻害剤とを組み合わせて投与することを特徴とする癌治療のための医薬 |
| UA123785C2 (uk) | 2016-03-28 | 2021-06-02 | Інсайт Корпорейшн | Сполуки піролотриазину як інгібітори tam |
| DK3481826T3 (da) | 2016-07-08 | 2022-01-10 | Rigel Pharmaceuticals Inc | Tyrosinkinaseinhibitorer |
| TWI704148B (zh) | 2016-10-10 | 2020-09-11 | 美商亞雷生物製藥股份有限公司 | 作為ｒｅｔ激酶抑制劑之經取代吡唑并[1,5-a]吡啶化合物 |
| JOP20190077A1 (ar) | 2016-10-10 | 2019-04-09 | Array Biopharma Inc | مركبات بيرازولو [1، 5-a]بيريدين بها استبدال كمثبطات كيناز ret |
| CN110267960B (zh) | 2017-01-18 | 2022-04-26 | 阿雷生物药品公司 | 作为RET激酶抑制剂的取代的吡唑并[1,5-a]吡嗪化合物 |
| WO2018136663A1 (fr) | 2017-01-18 | 2018-07-26 | Array Biopharma, Inc. | Inhibiteurs de ret |
| KR101794695B1 (ko) * | 2017-02-15 | 2017-11-07 | 한국바이오팜 주식회사 | 항염 효과가 우수한 기능성 식품 조성물 |
| JOP20190213A1 (ar) | 2017-03-16 | 2019-09-16 | Array Biopharma Inc | مركبات حلقية ضخمة كمثبطات لكيناز ros1 |
| JP7156287B2 (ja) | 2017-08-23 | 2022-10-19 | 小野薬品工業株式会社 | Ａｘｌ阻害剤を有効成分として含むがん治療剤 |
| PL3687996T3 (pl) | 2017-09-27 | 2022-02-21 | Incyte Corporation | Sole pochodnych pirolotriazyny użyteczne jako inhibitory tam |
| TWI876442B (zh) | 2017-10-10 | 2025-03-11 | 美商絡速藥業公司 | 6-(2-羥基-2-甲基丙氧基)-4-(6-(6-((6-甲氧基吡啶-3-基)甲基)-3,6-二氮雜雙環[3.1.1]庚-3-基)吡啶-3-基)吡唑并[1,5-a]吡啶-3-甲腈之調配物 |
| TWI791053B (zh) | 2017-10-10 | 2023-02-01 | 美商亞雷生物製藥股份有限公司 | 6-(2-羥基-2-甲基丙氧基)-4-(6-(6-((6-甲氧基吡啶-3-基)甲基)-3,6-二氮雜雙環[3.1.1]庚-3-基)吡啶-3-基)吡唑并[1,5-a]吡啶-3-甲腈之結晶形式及其醫藥組合物 |
| JP7223998B2 (ja) | 2017-10-13 | 2023-02-17 | 小野薬品工業株式会社 | Ａｘｌ阻害剤を有効成分として含む固形がん治療剤 |
| WO2019120121A1 (fr) * | 2017-12-21 | 2019-06-27 | 深圳市塔吉瑞生物医药有限公司 | Composé de diphénylaminopyrimidine inhibant l'activité de kinase |
| WO2019143991A1 (fr) | 2018-01-18 | 2019-07-25 | Array Biopharma Inc. | Composés de pyrazolo[3,4-d]pyrimidine substitués utilisés en tant qu'inhibiteurs de la kinase ret |
| US11603374B2 (en) | 2018-01-18 | 2023-03-14 | Array Biopharma Inc. | Substituted pyrrolo[2,3-d]pyrimidines compounds as ret kinase inhibitors |
| TW201932464A (zh) | 2018-01-18 | 2019-08-16 | 美商亞雷生物製藥股份有限公司 | 作為ret激酶抑制劑之經取代吡唑基[4,3-c]吡啶化合物 |
| WO2019195753A1 (fr) * | 2018-04-05 | 2019-10-10 | Tolero Pharmaceuticals, Inc. | Inhibiteurs de kinases axl et leur utilisation |
| US11442063B2 (en) | 2018-05-30 | 2022-09-13 | Promega Corporation | Broad spectrum kinase binding agents |
| EP4606432A3 (fr) | 2018-06-29 | 2025-10-29 | Incyte Corporation | Formulations d'un inhibiteur axl/mer |
| US11040038B2 (en) | 2018-07-26 | 2021-06-22 | Sumitomo Dainippon Pharma Oncology, Inc. | Methods for treating diseases associated with abnormal ACVR1 expression and ACVR1 inhibitors for use in the same |
| WO2020055672A1 (fr) | 2018-09-10 | 2020-03-19 | Array Biopharma Inc. | Composés hétérocycliques condensés comme inhibiteurs de kinases ret |
| US12257286B2 (en) | 2018-10-31 | 2025-03-25 | Mayo Foundation For Medical Education And Research | Methods and materials for treating cancer |
| EP3873500A4 (fr) | 2018-10-31 | 2023-01-11 | Mayo Foundation for Medical Education and Research | Méthodes et matériaux de traitement du cancer |
| BR112021018168B1 (pt) | 2019-03-21 | 2023-11-28 | Onxeo | Composição farmacêutica, combinação e kit compreendendo uma molécula dbait e um inibidor de quinase para o tratamento de câncer |
| JP2022539208A (ja) | 2019-07-03 | 2022-09-07 | スミトモ ファーマ オンコロジー， インコーポレイテッド | チロシンキナーゼ非受容体１（ｔｎｋ１）阻害剤およびその使用 |
| WO2021067772A1 (fr) * | 2019-10-04 | 2021-04-08 | Sumitomo Dainippon Pharma Oncology, Inc. | Formulations d'inhibiteur d'axl |
| CN114761006A (zh) | 2019-11-08 | 2022-07-15 | Inserm(法国国家健康医学研究院) | 对激酶抑制剂产生耐药性的癌症的治疗方法 |
| WO2021148581A1 (fr) | 2020-01-22 | 2021-07-29 | Onxeo | Nouvelle molécule dbait et son utilisation |
| AU2021230385A1 (en) | 2020-03-06 | 2022-09-22 | Incyte Corporation | Combination therapy comprising AXL/MER and PD-1/PD-L1 inhibitors |
| CN113061117B (zh) * | 2021-03-30 | 2023-02-10 | 长治学院 | 一种2-((5-氯-2-(4-吗啉甲基苯胺基)嘧啶-4-基)氨基)苯甲酰胺衍生物 |
| WO2022220227A1 (fr) * | 2021-04-14 | 2022-10-20 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | Composé de tétrahydropyridopyrimidine |
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| GB9523675D0 (en) | 1995-11-20 | 1996-01-24 | Celltech Therapeutics Ltd | Chemical compounds |
| GB9924862D0 (en) * | 1999-10-20 | 1999-12-22 | Celltech Therapeutics Ltd | Chemical compounds |
| GB0206215D0 (en) * | 2002-03-15 | 2002-05-01 | Novartis Ag | Organic compounds |
| GB0305929D0 (en) * | 2003-03-14 | 2003-04-23 | Novartis Ag | Organic compounds |
| AU2005233584B2 (en) * | 2004-04-09 | 2010-12-09 | Merck Sharp & Dohme Corp. | Inhibitors of Akt activity |
| US8133900B2 (en) * | 2005-11-01 | 2012-03-13 | Targegen, Inc. | Use of bi-aryl meta-pyrimidine inhibitors of kinases |
| PL1951684T3 (pl) * | 2005-11-01 | 2017-03-31 | Targegen, Inc. | Biarylowe meta-pirymidynowe inhibitory kinaz |
| WO2007056151A2 (fr) * | 2005-11-03 | 2007-05-18 | Irm Llc | Composes et compositions d’inhibiteurs de proteine kinases |
| EA200870217A1 (ru) * | 2006-01-30 | 2009-02-27 | Экселиксис, Инк. | 4-арил-2-аминопиримидины или 4-арил-2-аминоалкилпиримидины в качестве модуляторов jak-2 и содержащие их фармацевтические композиции |
| TW200902010A (en) * | 2007-01-26 | 2009-01-16 | Smithkline Beecham Corp | Anthranilamide inhibitors of aurora kinase |
| WO2008124085A2 (fr) * | 2007-04-03 | 2008-10-16 | Exelixis, Inc. | Méthodes d'utilisation de combinaisons d'inhibiteurs de mek et de jak-2 |
| EA017269B1 (ru) | 2007-05-04 | 2012-11-30 | Айрм Ллк | ПРОИЗВОДНЫЕ ПИРИМИДИНА И СОДЕРЖАЩИЕ ИХ КОМПОЗИЦИИ КАК ИНГИБИТОРЫ КИНАЗЫ c-kit И PDGFR |
| US8338439B2 (en) | 2008-06-27 | 2012-12-25 | Celgene Avilomics Research, Inc. | 2,4-disubstituted pyrimidines useful as kinase inhibitors |
| JP5802136B2 (ja) * | 2009-01-23 | 2015-10-28 | ライジェル ファーマシューティカルズ， インコーポレイテッド | Ｊａｋ経路の阻害のための組成物および方法 |
| AU2010210986A1 (en) * | 2009-02-09 | 2011-08-25 | Supergen, Inc. | Pyrrolopyrimidinyl Axl kinase inhibitors |
| US7741330B1 (en) | 2009-10-12 | 2010-06-22 | Pharmacyclics, Inc. | Pyrazolo-pyrimidine inhibitors of Bruton's tyrosine kinase |
| CN102791697A (zh) * | 2009-10-12 | 2012-11-21 | 瑞科西有限公司 | 作为TBKL和/或IKKε抑制剂的氨基-嘧啶化合物 |
| WO2012135641A2 (fr) * | 2011-03-30 | 2012-10-04 | H. Lee Moffitt Cancer Center And Research Institute | Inhibiteurs de kinase aurora et procédés pour les fabriquer et les utiliser |
| WO2012135800A1 (fr) | 2011-04-01 | 2012-10-04 | University Of Utah Research Foundation | Analogues de n-phénylpyrimidine-2-amine substitués en tant qu'inhibiteurs de l'axl kinase |
| EP2694486B1 (fr) | 2011-04-01 | 2018-01-10 | University of Utah Research Foundation | Analogues de n-(3-(pyrimidine-4-yl)phényl)acrylamide substitués en tant qu'inhibiteurs du récepteur tyrosine kinase btk |
-
2012
- 2012-03-31 WO PCT/US2012/031768 patent/WO2012135800A1/fr not_active Ceased
- 2012-03-31 EP EP19189727.1A patent/EP3628665B1/fr active Active
- 2012-03-31 BR BR112013025387-8A patent/BR112013025387B1/pt active IP Right Grant
- 2012-03-31 JP JP2014502897A patent/JP6118794B2/ja active Active
- 2012-03-31 ES ES19189727T patent/ES2937952T3/es active Active
- 2012-03-31 DK DK12763555T patent/DK2693881T3/da active
- 2012-03-31 ES ES12763555T patent/ES2759615T3/es active Active
- 2012-03-31 HU HUE12763555A patent/HUE046988T2/hu unknown
- 2012-03-31 PT PT127635555T patent/PT2693881T/pt unknown
- 2012-03-31 PL PL12763555T patent/PL2693881T3/pl unknown
- 2012-03-31 US US13/436,910 patent/US8901120B2/en active Active
- 2012-03-31 EP EP12763555.5A patent/EP2693881B1/fr active Active
-
2017
- 2017-02-03 JP JP2017018561A patent/JP2017075188A/ja not_active Withdrawn
-
2019
- 2019-12-03 CY CY20191101262T patent/CY1122556T1/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP2693881A1 (fr) | 2014-02-12 |
| WO2012135800A1 (fr) | 2012-10-04 |
| BR112013025387A2 (pt) | 2016-07-19 |
| EP2693881B1 (fr) | 2019-09-04 |
| JP2014509661A (ja) | 2014-04-21 |
| EP3628665B1 (fr) | 2022-11-02 |
| EP3628665A1 (fr) | 2020-04-01 |
| JP6118794B2 (ja) | 2017-04-19 |
| BR112013025387B1 (pt) | 2021-07-27 |
| DK2693881T3 (da) | 2019-12-09 |
| HUE046988T2 (hu) | 2020-04-28 |
| PT2693881T (pt) | 2019-12-09 |
| CY1122556T1 (el) | 2021-01-27 |
| US20120283261A1 (en) | 2012-11-08 |
| ES2937952T3 (es) | 2023-04-03 |
| EP2693881A4 (fr) | 2014-11-19 |
| US8901120B2 (en) | 2014-12-02 |
| ES2759615T3 (es) | 2020-05-11 |
| JP2017075188A (ja) | 2017-04-20 |
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